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FDA 510(k)

MiMo(TM) Negative Pressure Wound Therapy System

K-Number: K181929 · 2019-03-27

Decision Date2019-03-27
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MiMo(TM) Negative Pressure Wound Therapy System is a medical device manufactured by Baymax Research, Inc.. It received FDA 510(k) clearance on 2019-03-27 under approval number K181929. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MiMo(TM) Negative Pressure Wound Therapy System?

MiMo(TM) Negative Pressure Wound Therapy System is a medical device that received FDA 510(k) clearance on 2019-03-27. It is manufactured by Baymax Research, Inc.. The 510(k) number is K181929.

When was MiMo(TM) Negative Pressure Wound Therapy System approved by the FDA?

MiMo(TM) Negative Pressure Wound Therapy System received FDA 510(k) clearance on 2019-03-27, under approval number K181929.

What company makes MiMo(TM) Negative Pressure Wound Therapy System?

MiMo(TM) Negative Pressure Wound Therapy System is manufactured by Baymax Research, Inc..

What is the FDA product code for MiMo(TM) Negative Pressure Wound Therapy System?

The FDA product code for MiMo(TM) Negative Pressure Wound Therapy System is OMP.

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Official Source

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